Allele Registry

Canonical Allele Identifier: PA2825223628

Gene: TNNT2 HGNC NCBI

ClinVar RCV:

RCV000547266

ClinVar Variation:

469532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001431.1:p.Asp267Tyr	CA089206 NM_001001431.3:c.799G>T