Canonical Allele Identifier: PA2828704586
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 29819
ClinVar RCV Id: RCV000022695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364201.1:p.Cys167Arg
CA259668
NM_001377272.1:c.499T>C
CA2586972546
NM_001377272.1:c.498_499delinsTC