Canonical Allele Identifier: PA2829446452
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284110
ClinVar RCV Id: RCV000380276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp26900Gly
CA10604691
NM_003319.4:c.80699A>G