Canonical Allele Identifier: PA237840
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala20780Thr
CA237839
NM_133378.4:c.62338G>A