Canonical Allele Identifier: PA310718
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28364Gln
CA310716
NM_001267550.2:c.85091G>A