Canonical Allele Identifier: PA091565
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2136917
ClinVar RCV Id: RCV003037352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Glu272Lys
CA377509870
NM_000043.6:c.814G>A