Canonical Allele Identifier: PA2826554363
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 487631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Met1Ile
CA344209127
NM_001276345.2:c.3G>T
CA344209129
NM_001276345.2:c.3G>C
CA344209130
NM_001276345.2:c.3G>A