Canonical Allele Identifier: PA645411189
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26628Pro
CA1989422
NM_001267550.2:c.79883G>C