Canonical Allele Identifier: PA2830300893
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Asp239Val
CA126581
NM_152871.4:c.716A>T