rs201918850

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Species

Homo sapiens

Symbol

rs201918850

Category

Variant

Variant type

SNP

Overlaps

CPTP

Location

1:1327506

Nucleotide Change

G>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000001.11:g.1327506G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000343938.9:c.388G>A
• ENSEMBL:ENST00000464957.1:n.613G>A

HGVS.p name

• ENSP00000343890:p.Glu130Lys

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences