Allele Registry

Canonical Allele Identifier: PA093465

Gene: WNT4 HGNC NCBI

ClinVar RCV:

RCV000006691

ClinVar Variation:

6311

HGVS (amino-acid)	Matching Registered Transcripts
NP_110388.2:p.Leu12Pro	CA214934 NM_030761.5:c.35T>C