Canonical Allele Identifier: PA2826144190
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16395
ClinVar RCV Id: RCV000017821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171670.1:p.Leu143Gln
CA126450
NM_001184741.1:c.428T>A