Canonical Allele Identifier: PA2826555297
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404396
ClinVar RCV Id: RCV000476154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Glu136Asp
CA089006
NM_001276347.2:c.408G>T
CA344205883
NM_001276347.2:c.408G>C