Allele Registry

Canonical Allele Identifier: PA2828102084

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032177

RCV000513272

ClinVar Variation:

38926

444325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Pro254Ser	CA343191 NM_001363668.2:c.760_761delinsAG CA389225339 NM_001363668.2:c.760C>T