Canonical Allele Identifier: PA916005690
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43626
ClinVar RCV Id: RCV000036571 RCV000505760 RCV000556483 RCV000618563 RCV003450678 RCV003450679 RCV003450680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Asp96Ala
CA004228
NM_001276345.2:c.287A>C