Allele Registry

Canonical Allele Identifier: PA2829955736

Gene: WDR35 HGNC NCBI

ClinVar Variation Id: 288788

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Ile1156Arg	CA1542655 NM_020779.4:c.3467T>G