Allele Registry

Canonical Allele Identifier: PA261449

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000036570

RCV000825476

ClinVar Variation:

43625

666939

HGVS (amino-acid)	Matching Registered Transcripts
NP_000355.2:p.Asp98Glu	CA004247 NM_000364.3:c.294T>G CA344206634 NM_000364.3:c.294T>A