Canonical Allele Identifier: PA096558
Gene: WNT7A HGNC NCBI

Linked Data

ClinVar Variation Id: 40302
ClinVar RCV Id: RCV000033263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004616.2:p.Glu72Lys
CA130821
NM_004625.4:c.214G>A