Canonical Allele Identifier: PA658817182
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr34393Pro
CA60957488
NM_001267550.2:c.103177A>C