Canonical Allele Identifier: PA916065053
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg5566Cys
CA1995898
NM_133437.4:c.16696C>T