Canonical Allele Identifier: PA2825203969
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347811
ClinVar RCV Id: RCV000296696 RCV000334967 RCV001702008 RCV002520212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000499.1:p.Asp473Asn
CA3115087
NM_000508.5:c.1417G>A