Allele Registry

Canonical Allele Identifier: PA2825203999

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV004393924

ClinVar Variation:

3094587

HGVS (amino-acid)	Matching Registered Transcripts
NP_000499.1:p.Val726Ala	CA358523996 NM_000508.5:c.2177T>C