Allele Registry

Canonical Allele Identifier: PA113467

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000223859

ClinVar Variation:

235065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263274.1:p.Phe120Val	CA10581127 NM_001276345.2:c.358T>G