Canonical Allele Identifier: PA2826412638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg5047His
CA181933
NM_001256850.1:c.15140G>A