Canonical Allele Identifier: PA2829435489
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.His10911Tyr
CA178643
NM_003319.4:c.32731C>T