Canonical Allele Identifier: PA091576
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Tyr232Cys
CA126578
NM_000043.6:c.695A>G