Canonical Allele Identifier: PA309868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala6468Thr
CA309865
NM_133432.3:c.19402G>A