Allele Registry

Canonical Allele Identifier: PA343190

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032176

ClinVar Variation:

38925

HGVS (amino-acid)	Matching Registered Transcripts
NP_001092744.1:p.Phe288Leu	CA343189 NM_001099274.3:c.862T>C CA389225356 NM_001099274.3:c.864T>G CA389225360 NM_001099274.3:c.864T>A