Canonical Allele Identifier: PA2826419839
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19381His
CA178627
NM_001256850.1:c.58142G>A