Allele Registry

Canonical Allele Identifier: PA2829848555

Gene: WNT16 HGNC NCBI

ClinVar RCV:

RCV004199452

ClinVar Variation:

2363304

HGVS (amino-acid)	Matching Registered Transcripts
NP_057171.2:p.His77Gln	CA4455644 NM_016087.2:c.231C>G CA4455645 NM_016087.2:c.231C>A