Canonical Allele Identifier: PA645466201
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347818
ClinVar RCV Id: RCV000279650 RCV000371491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Gln206Glu
CA3115245
NM_021871.4:c.616C>G