Source: NC_000009.12:g.101476573C>A
Genes: PGAP4 (Hsa), TMEM246-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:101476573C>A