Allele Registry

Canonical Allele Identifier: PA645466209

Gene: FGA HGNC NCBI

ClinVar Allele:

297269

ClinVar RCV:

RCV000296696

RCV000334967

RCV001702008

RCV002520212

ClinVar Variation:

347811

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