Canonical Allele Identifier: PA2826555242
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43633
ClinVar RCV Id: RCV000036580 RCV004017308
ClinVar Variation Id: 229336
ClinVar RCV Id: RCV000220636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.His109Tyr
CA004375
NM_001276347.2:c.325C>T
CA10576373
NM_001276347.2:c.324_325delinsGT