Canonical Allele Identifier: PA645410272
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys18724Arg
CA1993298
NM_001267550.2:c.56171A>G