Canonical Allele Identifier: PA237902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191930
ClinVar RCV Id: RCV000172296 RCV000220034 RCV000283208 RCV000297539 RCV000401451 RCV000341926 RCV000400629 RCV000558110 RCV002453600 RCV004535172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20311Gln
CA237900
NM_001267550.2:c.60932G>A