Canonical Allele Identifier: PA2830300933
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 872244
ClinVar RCV Id: RCV001092604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Glu251Gly
CA377509875
NM_152871.4:c.752A>G