Canonical Allele Identifier: PA126605
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16513
ClinVar RCV Id: RCV000017977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Gly247Ala
CA126602
NM_000043.6:c.740G>C