Allele Registry

Canonical Allele Identifier: PA261451

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000036571

RCV000505760

RCV000556483

RCV000618563

RCV003450678

RCV003450679

RCV003450680

ClinVar Variation:

43626

HGVS (amino-acid)	Matching Registered Transcripts
NP_000355.2:p.Asp96Ala	CA004228 NM_000364.3:c.287A>C