Canonical Allele Identifier: PA2826555336
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499363
ClinVar RCV Id: RCV003221664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Arg156Ser
CA344204658
NM_001276347.2:c.468G>C
CA344204659
NM_001276347.2:c.468G>T