Canonical Allele Identifier: PA2829442697
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Cys22647Arg
CA358820
NM_003319.4:c.67939T>C