Canonical Allele Identifier: PA2573082744
Gene: WNT5A HGNC NCBI
ClinVar RCV:
RCV000577882
ClinVar Variation:
488060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003383.4:p.Ser160Cys
CA353275502
NM_003392.7:c.479C>G