Canonical Allele Identifier: PA2826144225
Gene: FGB HGNC NCBI

Linked Data

ClinVar Variation Id: 2498020
ClinVar RCV Id: RCV003219086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171670.1:p.Thr319Ile
CA358515231
NM_001184741.1:c.956C>T