Canonical Allele Identifier: PA2830222097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala19893Phe
CA310735
NM_133432.3:c.59677_59678delinsTT