Canonical Allele Identifier: PA658678961
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 466404
ClinVar RCV Id: RCV000558585 RCV001644651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006061.2:p.Thr364Pro
CA2517252
NM_006070.6:c.1090A>C