Canonical Allele Identifier: PA2830222200
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val20039Ile
CA302422
NM_133432.3:c.60115G>A