Canonical Allele Identifier: PA2830197050
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly17233Asp
CA1992669
NM_133378.4:c.51698G>A