Canonical Allele Identifier: PA2830300938
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2136917
ClinVar RCV Id: RCV003037352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Glu251Lys
CA377509870
NM_152871.4:c.751G>A