Allele Registry

Canonical Allele Identifier: PA343192

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032177

RCV000513272

ClinVar Variation:

38926

444325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092744.1:p.Pro289Ser	CA343191 NM_001099274.3:c.865_866delinsAG CA389225339 NM_001099274.3:c.865C>T