Canonical Allele Identifier: PA178289
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 165549
ClinVar RCV Id: RCV000152104 RCV000159282 RCV000533469 RCV000619541 RCV003453110 RCV003453111 RCV001193334 RCV003453109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg104Cys
CA004288
NM_000364.3:c.310C>T