Canonical Allele Identifier: PA2830223784
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg22488Ser
CA310944
NM_133432.3:c.67462C>A