Allele Registry

Canonical Allele Identifier: PA2828102075

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032172

ClinVar Variation:

38921

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Pro248His	CA343182 NM_001363668.2:c.743C>A