Canonical Allele Identifier: PA2580470813
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2096855
ClinVar RCV Id: RCV003006212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg408His
CA65919439
NM_025216.3:c.1223G>A