Canonical Allele Identifier: PA916005689
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Arg94Ser
CA004222
NM_001276345.2:c.282A>T
CA344206659
NM_001276345.2:c.282A>C