Canonical Allele Identifier: PA178641
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165922
ClinVar RCV Id: RCV000152267 RCV000535645 RCV000714063 RCV001128979 RCV001128975 RCV001128976 RCV001128977 RCV001128978 RCV002453496 RCV003486676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys17862Tyr
CA178640
NM_133378.4:c.53585G>A