Canonical Allele Identifier: PA2828918687
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 1308334
ClinVar RCV Id: RCV001763246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369688.1:p.Tyr331Cys
CA358515201
NM_001382759.1:c.992A>G