Canonical Allele Identifier: PA2826422129
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg23411His
CA235074
NM_001256850.1:c.70232G>A