Canonical Allele Identifier: PA2829432385
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg5252Pro
CA309802
NM_003319.4:c.15755G>C