Canonical Allele Identifier: PA2830200689
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 519091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg25871Trp
CA1988664
NM_133378.4:c.77611C>T