Allele Registry

Canonical Allele Identifier: PA112770

Gene: TFG HGNC NCBI

ClinVar RCV:

RCV000087273

RCV001038327

RCV001549766

RCV002321583

ClinVar Variation:

100909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001007566.1:p.Arg106Cys	CA150664 NM_001007565.2:c.316C>T