Canonical Allele Identifier: PA310883
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg30467Cys
CA310881
NM_001267550.2:c.91399C>T