Allele Registry

Canonical Allele Identifier: PA645466211

Gene: FGA HGNC NCBI

ClinVar Allele:

297256

ClinVar RCV:

RCV000350523

RCV000388685

RCV002502338

ClinVar Variation:

347810

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.Val482Met	CA3115086 NM_021871.4:c.1444G>A