Canonical Allele Identifier: PA2830217230
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asp11871Gly
CA310206
NM_133432.3:c.35612A>G