Canonical Allele Identifier: PA2826371755
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 162612
ClinVar RCV Id: RCV000169740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243034.1:p.Tyr71Cys
CA346838
NM_001256105.1:c.212A>G