Canonical Allele Identifier: PA2830240331
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Trp22856Cys
CA358826
NM_133437.4:c.68568G>C
CA349464189
NM_133437.4:c.68568G>T