Allele Registry

Canonical Allele Identifier: PA130228

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV000030941

RCV000851581

RCV000851971

RCV001509236

RCV002228034

RCV002476987

RCV004532379

ClinVar Variation:

16404

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.Arg35His	CA130224 NM_021871.4:c.104G>A