Canonical Allele Identifier: PA2830203982
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys32219Glu
CA1985434
NM_133378.4:c.96655A>G