Canonical Allele Identifier: PA237841
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala23348Thr
CA237839
NM_001267550.2:c.70042G>A