Canonical Allele Identifier: PA658816173
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys27483Arg
CA60987026
NM_001267550.2:c.82448A>G