Allele Registry

Canonical Allele Identifier: PA645466216

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV000323812

RCV000381748

RCV004021942

ClinVar Variation:

347807

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.His613Arg	CA3115024 NM_021871.4:c.1838A>G