Source: NC_000001.11:g.152409878C>T
Genes: CRNN (Hsa), CCDST (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:152409878C>T