Canonical Allele Identifier: PA2826555369
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_001263276.1:p.Ala172Ser
CA004712
NM_001276347.2:c.514G>T