Allele Registry

Canonical Allele Identifier: PA891856069

Gene: WNT10A HGNC NCBI

ClinVar Variation Id: 582506

HGVS (amino-acid)	Matching Registered Transcripts
NP_079492.2:p.Arg69Trp	CA2113856 NM_025216.3:c.205C>T