Canonical Allele Identifier: PA2829446278
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu26731Ala
CA349401143
NM_003319.4:c.80192A>C