Canonical Allele Identifier: PA2830191462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg2540Cys
CA2004773
NM_133378.4:c.7618C>T