Canonical Allele Identifier: PA302838
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 195636
ClinVar RCV Id: RCV000222990 RCV000643008 RCV000724717 RCV001134131 RCV001134132 RCV001134128 RCV001134130 RCV001134129 RCV002426845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg14750Gln
CA302836
NM_001256850.1:c.44249G>A