Allele Registry

Canonical Allele Identifier: PA2580124802

Gene: FGA HGNC NCBI

ClinVar RCV:

RCV002684893

ClinVar Variation:

2385030

HGVS (amino-acid)	Matching Registered Transcripts
NP_000499.1:p.His780Gln	CA3114887 NM_000508.5:c.2340C>A CA358523265 NM_000508.5:c.2340C>G