Allele Registry

Canonical Allele Identifier: PA2499295700

Gene: WNT7B HGNC NCBI

ClinVar Allele:

1289409

ClinVar RCV:

RCV001728160

ClinVar Variation:

1299462

HGVS (amino-acid)	Matching Registered Transcripts
NP_478679.1:p.Gly188Ser	CA411901516 NM_058238.3:c.562G>A