Canonical Allele Identifier: PA2826371803
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 29819
ClinVar RCV Id: RCV000022695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243034.1:p.Cys167Arg
CA259668
NM_001256105.1:c.499T>C
CA2586972546
NM_001256105.1:c.498_499delinsTC