Canonical Allele Identifier: PA2830215026
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile7967Val
CA309977
NM_133432.3:c.23899A>G