Canonical Allele Identifier: PA179434
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ala405Thr
CA179430
NM_133379.5:c.1213G>A