Canonical Allele Identifier: PA126519
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 16420
ClinVar RCV Id: RCV000017882 RCV000338448 RCV000246757 RCV000405212 RCV001509235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068657.1:p.Thr331Ala
CA126515
NM_021871.4:c.991A>G