Canonical Allele Identifier: PA132847
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43640
ClinVar RCV Id: RCV000036588 RCV000845416 RCV001171164 RCV001222522 RCV000505718 RCV003298061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Arg139Cys
CA004505
NM_001001430.3:c.415C>T