Allele Registry

Canonical Allele Identifier: PA2828102029

Gene: TINF2 HGNC NCBI

ClinVar RCV:

RCV000032163

RCV000303934

RCV000347889

RCV000399248

RCV000862737

RCV003914887

ClinVar Variation:

38915

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Pro201Ser	CA343170 NM_001363668.2:c.601C>T