Canonical Allele Identifier: PA916066931
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr9587Ile
CA310092
NM_133437.4:c.28760C>T