Allele Registry

Canonical Allele Identifier: PA2828102087

Gene: TINF2 HGNC NCBI

ClinVar Allele:

47530

ClinVar RCV:

RCV000032178

ClinVar Variation:

38927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Arg256Gly	CA343193 NM_001363668.2:c.766A>G