Canonical Allele Identifier: PA178635
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165915
ClinVar RCV Id: RCV000152264 RCV000300379 RCV000339294 RCV000304060 RCV000392749 RCV000400185 RCV000869565 RCV001704099 RCV002336306 RCV003486675
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu19118Lys
CA178633
NM_001256850.1:c.57352G>A