Canonical Allele Identifier: PA183680
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Phe32806Tyr
CA183679
NM_133378.4:c.98417T>A