Canonical Allele Identifier: PA2829429622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys566Glu
CA185553
NM_003319.4:c.1696A>G