Canonical Allele Identifier: PA100135
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16390
ClinVar RCV Id: RCV000017816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005132.2:p.Gly430Asp
CA126444
NM_005141.5:c.1289G>A