Allele Registry

Canonical Allele Identifier: PA113441

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000036615

RCV000148901

RCV000225695

RCV000415651

RCV000415695

RCV000777715

RCV000778959

RCV000793380

RCV002381298

ClinVar Variation:

43667

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263274.1:p.Glu254Asp	CA090003 NM_001276345.2:c.762G>T CA344202697 NM_001276345.2:c.762G>C