Canonical Allele Identifier: PA2828918928
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 1308334
ClinVar RCV Id: RCV001763246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369691.1:p.Tyr275Cys
CA358515201
NM_001382762.1:c.824A>G