Canonical Allele Identifier: PA2826412822
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg5426Gln
CA2001876
NM_001256850.1:c.16277G>A