Canonical Allele Identifier: PA2830211371
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497010
ClinVar RCV Id: RCV000592201 RCV001128781 RCV001131430 RCV001131431 RCV001131432 RCV001128780 RCV001170106 RCV002367996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg2074Gln
CA2005064
NM_133432.3:c.6221G>A