Canonical Allele Identifier: PA2826420169
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19963Gln
CA183598
NM_001256850.1:c.59888G>A