Canonical Allele Identifier: PA141611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47652
ClinVar RCV Id: RCV000040921 RCV000082470 RCV000622061 RCV000852775 RCV001130524 RCV001130525 RCV001130527 RCV001080039 RCV001130526 RCV001130528
ClinVar Variation Id: 796406
ClinVar RCV Id: RCV000979793
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile31631Val
CA141609
NM_133378.4:c.94891A>G
CA915942139
NM_133378.4:c.94890_94891delinsTG