Canonical Allele Identifier: PA139132
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46759
ClinVar RCV Id: RCV000040029 RCV000082380 RCV000280234 RCV000293034 RCV000387544 RCV000333108 RCV000374655 RCV000852888 RCV001082276 RCV001798137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg8497His
CA139128
NM_001267550.2:c.25490G>A