Canonical Allele Identifier: PA2741992755
Gene: WNT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2785066
ClinVar RCV Id: RCV003662623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110388.2:p.Cys43Tyr
CA675507
NM_030761.5:c.128G>A