Canonical Allele Identifier: PA358037
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202730
ClinVar RCV Id: RCV000210582 RCV000725154 RCV001079720 RCV001133603 RCV001133604 RCV001133605 RCV001135094 RCV001133602 RCV001170370 RCV002444754 RCV003226239 RCV004537548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile16648Val
CA310110
NM_133378.4:c.49942A>G