Allele Registry

Canonical Allele Identifier: PA272798

Gene: WDR62 HGNC NCBI

ClinVar RCV:

RCV000147962

ClinVar Variation:

160292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001077430.1:p.Ser120Tyr	CA272797 NM_001083961.2:c.359C>A