Canonical Allele Identifier: PA309682
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg11524Gln
CA309680
NM_001267550.2:c.34571G>A