Allele Registry

Canonical Allele Identifier: PA132892

Gene: TNNT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000036626

RCV000148899

RCV000223838

RCV000245252

RCV000459071

RCV001187862

RCV003450726

RCV003450727

RCV003450728

ClinVar Variation:

43677

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000355.2:p.Arg293His	CA005304 NM_000364.3:c.878G>A