Canonical Allele Identifier: PA1139698031
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 919022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg140His
CA344205960
NM_001276345.2:c.419G>A