Canonical Allele Identifier: PA100147
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_005132.2:p.Leu202Gln
CA126450
NM_005141.5:c.605T>A