Allele Registry

Canonical Allele Identifier: PA126518

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV000017882

RCV000246757

RCV000338448

RCV000405212

RCV001509235

ClinVar Variation:

16420

HGVS (amino-acid)	Matching Registered Transcripts
NP_000499.1:p.Thr331Ala	CA126515 NM_000508.5:c.991A>G