Canonical Allele Identifier: PA140742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg22789His
CA140740
NM_133378.4:c.68366G>A