Allele Registry

Canonical Allele Identifier: PA2826371755

Gene: WNT5A HGNC NCBI

ClinVar RCV:

RCV000169740

ClinVar Variation:

162612

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243034.1:p.Tyr71Cys	CA346838 NM_001256105.1:c.212A>G