Allele Registry

Canonical Allele Identifier: PA2825203906

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV000279650

RCV000371491

ClinVar Variation:

347818

HGVS (amino-acid)	Matching Registered Transcripts
NP_000499.1:p.Gln206Glu	CA3115245 NM_000508.5:c.616C>G