Canonical Allele Identifier: PA2828919065
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16387
ClinVar RCV Id: RCV000017811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369693.1:p.Ala98Thr
CA126440
NM_001382764.1:c.292G>A