Canonical Allele Identifier: PA308966
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala744Thr
CA308962
NM_133379.5:c.2230G>A