Allele Registry

Canonical Allele Identifier: PA096524

Gene: WNT7A HGNC NCBI

ClinVar Allele:

23100

ClinVar RCV:

RCV000008527

ClinVar Variation:

8061

HGVS (amino-acid)	Matching Registered Transcripts
NP_004616.2:p.Ala109Thr	CA119262 NM_004625.4:c.325G>A