Canonical Allele Identifier: PA139986
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47093
ClinVar RCV Id: RCV000040363 RCV000461813 RCV001131522 RCV001131523 RCV001131524 RCV001131525 RCV001131526 RCV001699025 RCV002433514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val15661Met
CA139984
NM_133378.4:c.46981G>A