Canonical Allele Identifier: PA658666795
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg23767Gln
CA1990652
NM_001267550.2:c.71300G>A