Allele Registry

Canonical Allele Identifier: PA2828102071

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032167

RCV000319654

RCV000372254

RCV000868533

RCV000989196

RCV001818201

ClinVar Variation:

38918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Glu246Lys	CA343176 NM_001363668.2:c.736G>A