Canonical Allele Identifier: PA2830191613
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile2969Val
CA2004477
NM_133378.4:c.8905A>G