Canonical Allele Identifier: PA214933
Gene: WNT4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6310
ClinVar RCV Id: RCV000006690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110388.2:p.Arg83Trp
CA214932
NM_030761.5:c.247C>T