Canonical Allele Identifier: PA091564
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 872244
ClinVar RCV Id: RCV001092604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Glu272Gly
CA377509875
NM_000043.6:c.815A>G