Canonical Allele Identifier: PA2826440966
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys18618Arg
CA1993375
NM_001267550.2:c.55852T>C