Canonical Allele Identifier: PA2826555363
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181621
ClinVar RCV Id: RCV000159302 RCV001089605 RCV003453228 RCV003453227 RCV003453229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Asn164Lys
CA004658
NM_001276347.2:c.492C>A
CA344204517
NM_001276347.2:c.492C>G