Canonical Allele Identifier: PA140478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47256
ClinVar RCV Id: RCV000040526 RCV000172726 RCV000243819 RCV001085386 RCV001135884 RCV001135885 RCV001135886 RCV001135887 RCV001135883 RCV002225279 RCV003149655 RCV003993766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg1998His
CA140473
NM_133378.4:c.5993G>A