Canonical Allele Identifier: PA645397458
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 301531
ClinVar RCV Id: RCV000337266 RCV003343765
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Glu289Asp
CA5593228
NM_000043.6:c.867A>C
CA377509995
NM_000043.6:c.867A>T