Canonical Allele Identifier: PA181601
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg29980Cys
CA181600
NM_133378.4:c.89938C>T