Canonical Allele Identifier: PA645410664
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg22058Cys
CA1991556
NM_001267550.2:c.66172C>T