Allele Registry

Canonical Allele Identifier: PA2826202447

Gene: TFG HGNC NCBI

ClinVar RCV:

RCV000144505

ClinVar Variation:

156445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182407.1:p.Gly269Val	CA170881 NM_001195478.2:c.806G>T