Allele Registry

Canonical Allele Identifier: PA261458

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000036581

ClinVar Variation:

43634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001430.1:p.Glu118Lys	CA004396 NM_001001430.3:c.352G>A