Canonical Allele Identifier: PA2829442402
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys22203Thr
CA183580
NM_003319.4:c.66608A>C