Canonical Allele Identifier: PA2825203934
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 347813
ClinVar RCV Id: RCV000303506 RCV000360629 RCV002520213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000499.1:p.Asn307Asp
CA3115196
NM_000508.5:c.919A>G