Allele Registry

Canonical Allele Identifier: PA645466215

Gene: FGA HGNC NCBI

ClinVar Allele:

297349

ClinVar RCV:

RCV000270905

RCV000328375

RCV002520211

ClinVar Variation:

347808

HGVS (amino-acid)	Matching Registered Transcripts
NP_068657.1:p.Gly608Ala	CA3115027 NM_021871.4:c.1823G>C