Canonical Allele Identifier: PA2829955498
Gene: WDR35 HGNC NCBI

Linked Data

ClinVar Variation Id: 437865
ClinVar RCV Id: RCV000504572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065830.2:p.Arg461Gln
CA1543248
NM_020779.4:c.1382G>A