Canonical Allele Identifier: PA2830200856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala26265Phe
CA310735
NM_133378.4:c.78793_78794delinsTT