Canonical Allele Identifier: PA2830031013
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3190701
ClinVar RCV Id: RCV004483109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg77His
CA2113864
NM_025216.3:c.230G>A