Canonical Allele Identifier: PA2825203886
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347822
ClinVar RCV Id: RCV000344051 RCV000404726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000499.1:p.Thr82Pro
CA3115349
NM_000508.5:c.244A>C