Canonical Allele Identifier: PA2830218818
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg14448Gln
CA310394
NM_133432.3:c.43343G>A