Canonical Allele Identifier: PA100157
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 16389
ClinVar RCV Id: RCV000017815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005132.2:p.Leu383Arg
CA126442
NM_005141.5:c.1148T>G