Canonical Allele Identifier: PA302458
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191923
ClinVar RCV Id: RCV000172288 RCV000559196 RCV000769981 RCV001135230 RCV001135229 RCV001135226 RCV001135227 RCV001135228 RCV002453599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp18725Asn
CA302457
NM_133378.4:c.56173G>A