Canonical Allele Identifier: PA2830223996
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Trp22789Cys
CA358826
NM_133432.3:c.68367G>C
CA349464189
NM_133432.3:c.68367G>T