Canonical Allele Identifier: PA2830204054
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32291Trp
CA60956099
NM_133378.4:c.96871C>T