Allele Registry

Canonical Allele Identifier: PA2826202728

Gene: TFG HGNC NCBI

ClinVar RCV:

RCV000030736

RCV000218755

RCV000642397

RCV001095428

RCV002251934

ClinVar Variation:

37089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182408.1:p.Pro281Leu	CA130077 NM_001195479.2:c.842C>T