Canonical Allele Identifier: PA178573
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165880
ClinVar RCV Id: RCV000152243 RCV000552973 RCV002354350 RCV001704098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg22482Gln
CA178570
NM_001267550.2:c.67445G>A