Canonical Allele Identifier: PA096538
Gene: WNT7A HGNC NCBI

Linked Data

ClinVar Variation Id: 40130
ClinVar RCV Id: RCV000033175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004616.2:p.Arg222Trp
CA130747
NM_004625.4:c.664C>T