Allele Registry

Canonical Allele Identifier: PA2826554775

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV001756730

ClinVar Variation:

1303231

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263275.1:p.Arg100Gly	CA344205964 NM_001276346.2:c.298C>G