Canonical Allele Identifier: PA212973
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16508
ClinVar RCV Id: RCV000017972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Ala25Thr
CA212971
NM_000043.6:c.73G>A