Allele Registry

Canonical Allele Identifier: PA916012082

Gene: TFG HGNC NCBI

ClinVar RCV:

RCV000144505

ClinVar Variation:

156445

HGVS (amino-acid)	Matching Registered Transcripts
NP_006061.2:p.Gly269Val	CA170881 NM_006070.6:c.806G>T