Canonical Allele Identifier: PA2830228765
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala697Val
CA256505
NM_133437.4:c.2090C>T