Allele Registry

Canonical Allele Identifier: PA126497

Gene: FGA HGNC NCBI

ClinVar Allele:

31449

ClinVar RCV:

RCV000017871

RCV002490381

RCV003480033

ClinVar Variation:

16410

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.Glu545Val	CA126494 NM_021871.4:c.1634A>T