Canonical Allele Identifier: PA2573290329
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1466056
ClinVar RCV Id: RCV001963872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Met1Leu