Canonical Allele Identifier: PA2828704397
Gene: WNT5A HGNC NCBI

Linked Data

ClinVar Variation Id: 29820
ClinVar RCV Id: RCV000022696
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364200.1:p.Cys68Ser
CA342716
NM_001377271.1:c.203G>C
CA353267396
NM_001377271.1:c.202T>A