Canonical Allele Identifier: PA2830218803
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val14426Ala
CA302906
NM_133432.3:c.43277T>C