Allele Registry

Canonical Allele Identifier: PA2829955518

Gene: WDR35 HGNC NCBI

ClinVar RCV:

RCV000055831

ClinVar Variation:

65620

HGVS (amino-acid)	Matching Registered Transcripts
NP_065830.2:p.Leu520Pro	CA344943 NM_020779.4:c.1559T>C