Canonical Allele Identifier: PA2829445877
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Phe26309Tyr
CA183679
NM_003319.4:c.78926T>A