Allele Registry

Canonical Allele Identifier: PA2826202778

Gene: TFG HGNC NCBI

ClinVar Allele:

244402

ClinVar RCV:

RCV000235479

RCV000533138

RCV001081716

RCV002411066

ClinVar Variation:

245772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182408.1:p.Pro350Ala	CA2517248 NM_001195479.2:c.1048C>G