Canonical Allele Identifier: PA2830227161
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Phe26434Tyr
CA183679
NM_133432.3:c.79301T>A