Canonical Allele Identifier: PA2830218242
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val13464Met
CA1991353
NM_133432.3:c.40390G>A