Canonical Allele Identifier: PA2826371752
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_001243034.1:p.Cys68Ser
CA342716
NM_001256105.1:c.203G>C
CA353267396
NM_001256105.1:c.202T>A