Allele Registry

Canonical Allele Identifier: PA113377

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013225

RCV000157537

RCV000159296

RCV000211866

RCV000524542

RCV000710045

RCV001375512

RCV003225021

RCV003450628

RCV003450629

ClinVar Variation:

12414

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263274.1:p.Arg151Trp	CA004526 NM_001276345.2:c.451C>T