Canonical Allele Identifier: PA2828919019
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16383
ClinVar RCV Id: RCV000017807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369692.1:p.Ala362Thr
CA126431
NM_001382763.1:c.1084G>A