Allele Registry

Canonical Allele Identifier: PA2828102082

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032176

ClinVar Variation:

38925

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Phe253Leu	CA343189 NM_001363668.2:c.757T>C CA389225356 NM_001363668.2:c.759T>G CA389225360 NM_001363668.2:c.759T>A