Canonical Allele Identifier: PA181631
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178169
ClinVar RCV Id: RCV000154892 RCV000458064 RCV000620291 RCV000725299 RCV001133267 RCV001133263 RCV001133264 RCV001133266 RCV001133265 RCV002467607 RCV003149943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile30899Thr
CA181628
NM_001267550.2:c.92696T>C