Allele Registry

Canonical Allele Identifier: PA645506992

Gene: TFG HGNC NCBI

ClinVar Allele:

244402

ClinVar RCV:

RCV000235479

RCV000533138

RCV001081716

RCV002411066

ClinVar Variation:

245772

HGVS (amino-acid)	Matching Registered Transcripts
NP_006061.2:p.Pro354Ala	CA2517248 NM_006070.6:c.1060C>G