Canonical Allele Identifier: PA2829446362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Lys26821Arg
CA183096
NM_003319.4:c.80462A>G