Canonical Allele Identifier: PA179027
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_597676.3:p.Cys4059Gly
CA179026
NM_133432.3:c.12175T>G