Canonical Allele Identifier: PA132835
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43623
ClinVar RCV Id: RCV000036568 RCV000244818 RCV001293092 RCV000159277 RCV001798103 RCV001366540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg94Thr
CA004216
NM_000364.3:c.281G>C