Canonical Allele Identifier: PA658678957
Gene: TFG HGNC NCBI

Linked Data

ClinVar Variation Id: 466412
ClinVar RCV Id: RCV001755843 RCV000554884 RCV002384150
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006061.2:p.Thr330Ala
CA2517240
NM_006070.6:c.988A>G