Allele Registry

Canonical Allele Identifier: PA2828102076

Gene: TINF2 HGNC NCBI

ClinVar Allele:

47522

ClinVar RCV:

RCV000032170

ClinVar Variation:

38919

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Pro248Ala	CA343178 NM_001363668.2:c.742C>G