Canonical Allele Identifier: PA2830214023
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile6131Thr
CA309841
NM_133432.3:c.18392T>C