Canonical Allele Identifier: PA2829454136
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 162612
ClinVar RCV Id: RCV000169740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003383.4:p.Tyr86Cys
CA346838
NM_003392.7:c.257A>G