Allele Registry

Canonical Allele Identifier: PA2828102113

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV003861457

ClinVar Variation:

3006842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Met283Ile	CA389224256 NM_001363668.2:c.849G>C CA389224264 NM_001363668.2:c.849G>A CA389224274 NM_001363668.2:c.849G>T