Canonical Allele Identifier: PA2828704399
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 162612
ClinVar RCV Id: RCV000169740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364200.1:p.Tyr71Cys
CA346838
NM_001377271.1:c.212A>G