Canonical Allele Identifier: PA2826371749
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 162613
ClinVar RCV Id: RCV000169741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243034.1:p.Cys54Tyr
CA346840
NM_001256105.1:c.161G>A