Allele Registry

Canonical Allele Identifier: PA261453

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000159280

RCV000208103

RCV000474512

RCV000620701

RCV000768491

RCV001807762

RCV003450681

RCV003450682

RCV003486557

RCV004525863

RCV004541099

ClinVar Variation:

43627

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001430.1:p.Arg92Trp	CA004266 NM_001001430.3:c.274C>T