Canonical Allele Identifier: PA179028
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166235
ClinVar RCV Id: RCV000152418 RCV000643407 RCV002326875 RCV001358499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys4297Gly
CA179026
NM_001267550.2:c.12889T>G