Allele Registry

Canonical Allele Identifier: PA2828102073

Gene: TINF2 HGNC NCBI

ClinVar Allele:

20666

ClinVar RCV:

RCV000005981

RCV000032169

RCV000434257

RCV001054196

ClinVar Variation:

5627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Arg247Cys	CA117653 NM_001363668.2:c.739C>T