Canonical Allele Identifier: PA2825224567
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177807
ClinVar RCV Id: RCV000159288 RCV000211744 RCV000824804 RCV001089627 RCV003453157 RCV003453159 RCV003453158 RCV003531982 RCV003764947
ClinVar Variation Id: 235064
ClinVar RCV Id: RCV000223771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Phe105Leu
CA004389
NM_001001432.3:c.315T>G
CA10581128
NM_001001432.3:c.313T>C
CA344206365
NM_001001432.3:c.315T>A