Canonical Allele Identifier: PA2826144221
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_001171670.1:p.Ala306Thr
CA126431
NM_001184741.1:c.916G>A