Canonical Allele Identifier: PA2830238429
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala19960Phe
CA310735
NM_133437.4:c.59878_59879delinsTT