Canonical Allele Identifier: PA658803976
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 523628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000499.1:p.Gly697Ser
CA3114940
NM_000508.5:c.2089G>A