Canonical Allele Identifier: PA126501
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 16411
ClinVar RCV Id: RCV000017872 RCV002222001 RCV002490382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Arg573Cys
CA126498
NM_021871.4:c.1717C>T