Canonical Allele Identifier: PA183097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys33318Arg
CA183096
NM_133378.4:c.99953A>G