Allele Registry

Canonical Allele Identifier: PA2580306278

Gene: WNT7A HGNC NCBI

ClinVar RCV:

RCV002621599

RCV003348870

ClinVar Variation:

1922392

HGVS (amino-acid)	Matching Registered Transcripts
NP_004616.2:p.Tyr313His	CA2266325 NM_004625.4:c.937T>C