Canonical Allele Identifier: PA126497
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 16410
ClinVar RCV Id: RCV000017871 RCV002490381 RCV003480033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Glu545Val
CA126494
NM_021871.4:c.1634A>T