Canonical Allele Identifier: PA2829454122
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 29820
ClinVar RCV Id: RCV000022696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003383.4:p.Cys83Ser
CA342716
NM_003392.7:c.248G>C
CA353267396
NM_003392.7:c.247T>A