Canonical Allele Identifier: PA2828704447
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 29819
ClinVar RCV Id: RCV000022695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364200.1:p.Cys167Arg
CA259668
NM_001377271.1:c.499T>C
CA2586972546
NM_001377271.1:c.498_499delinsTC