Canonical Allele Identifier: PA916005813
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 181612
ClinVar RCV Id: RCV000615596 RCV000778960 RCV001067821 RCV001101098 RCV001101099 RCV001185278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Ala182Ser
CA004712
NM_001276345.2:c.544G>T