Canonical Allele Identifier: PA297430
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Asn164Lys
CA004658
NM_001001430.3:c.492C>A
CA344204517
NM_001001430.3:c.492C>G