Allele Registry

Canonical Allele Identifier: PA261459

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000036581

ClinVar Variation:

43634

HGVS (amino-acid)	Matching Registered Transcripts
NP_000355.2:p.Glu128Lys	CA004396 NM_000364.3:c.382G>A