Allele Registry

Canonical Allele Identifier: PA2826202762

Gene: TFG HGNC NCBI

ClinVar Allele:

451907

ClinVar RCV:

RCV000554884

RCV001755843

RCV002384150

ClinVar Variation:

466412

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182408.1:p.Thr326Ala	CA2517240 NM_001195479.2:c.976A>G