Allele Registry

Canonical Allele Identifier: PA645506990

Gene: TFG HGNC NCBI

ClinVar RCV:

RCV000030736

RCV000218755

RCV000642397

RCV001095428

RCV002251934

ClinVar Variation:

37089

HGVS (amino-acid)	Matching Registered Transcripts
NP_006061.2:p.Pro285Leu	CA130077 NM_006070.6:c.854C>T