Allele Registry

Canonical Allele Identifier: PA2828102037

Gene: TINF2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

47519

ClinVar RCV:

RCV000032164

RCV000350321

RCV000394153

RCV000545340

RCV001269497

RCV001731323

RCV002496488

ClinVar Variation:

38916

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350597.1:p.Ser210Tyr	CA343172 NM_001363668.2:c.629C>A