Canonical Allele Identifier: PA2827512999
Gene: DDX59 HGNC NCBI

Linked Data

ClinVar Variation Id: 88653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336728.1:p.Val367Gly
CA145273
NM_001349799.3:c.1100T>G