Canonical Allele Identifier: PA181671
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178178
ClinVar RCV Id: RCV000154905 RCV000264981 RCV000389752 RCV000270733 RCV000384089 RCV000329578 RCV000457318 RCV002354368 RCV004534969
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met29046Arg
CA181669
NM_001267550.2:c.87137T>G