Canonical Allele Identifier: PA096545
Gene: WNT7A HGNC NCBI

Linked Data

ClinVar Variation Id: 8060
ClinVar RCV Id: RCV000008526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004616.2:p.Arg292Cys
CA119261
NM_004625.4:c.874C>T