Canonical Allele Identifier: PA2826554750
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181611
ClinVar RCV Id: RCV000159273 RCV001798538 RCV003453216 RCV001850238 RCV003453217 RCV003453215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Pro89Thr
CA004164
NM_001276346.2:c.265C>A