Allele Registry

Canonical Allele Identifier: PA2580500821

Gene: WNT16 HGNC NCBI

ClinVar RCV:

RCV004199452

ClinVar Variation:

2363304

HGVS (amino-acid)	Matching Registered Transcripts
NP_476509.1:p.His87Gln	CA4455644 NM_057168.2:c.261C>G CA4455645 NM_057168.2:c.261C>A