Canonical Allele Identifier: PA096524
Gene: WNT7A HGNC NCBI

Linked Data

ClinVar Variation Id: 8061
ClinVar RCV Id: RCV000008527
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004616.2:p.Ala109Thr
CA119262
NM_004625.4:c.325G>A