Canonical Allele Identifier: PA2829432967
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ala6343Thr
CA309865
NM_003319.4:c.19027G>A