Canonical Allele Identifier: PA645466209
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347811
ClinVar RCV Id: RCV000296696 RCV000334967 RCV001702008 RCV002520212
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Asp473Asn
CA3115087
NM_021871.4:c.1417G>A