Canonical Allele Identifier: PA178636
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165915
ClinVar RCV Id: RCV000152264 RCV000300379 RCV000339294 RCV000304060 RCV000392749 RCV000400185 RCV000869565 RCV001704099 RCV002336306 RCV003486675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu20759Lys
CA178633
NM_001267550.2:c.62275G>A