Canonical Allele Identifier: PA200181
Gene: WNT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 189347
ClinVar RCV Id: RCV000172899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110380.1:p.Cys91Arg
CA200180
NM_030753.5:c.271T>C