Canonical Allele Identifier: PA2830222392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg20353His
CA181666
NM_133432.3:c.61058G>A