Canonical Allele Identifier: PA2826421031
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg21443Gln
CA1990959
NM_001256850.1:c.64328G>A