Allele Registry

Canonical Allele Identifier: PA645506989

Gene: TFG HGNC NCBI

ClinVar Variation Id: 432643

HGVS (amino-acid)	Matching Registered Transcripts
NP_006061.2:p.Ser8Arg	CA353836672 NM_006070.6:c.22A>C CA353836678 NM_006070.6:c.24T>A CA353836679 NM_006070.6:c.24T>G