Canonical Allele Identifier: PA2826554479
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181637
ClinVar RCV Id: RCV000159330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.His101_Arg102insLeu
CA004260
NM_001276345.2:c.304_305insTTC