Canonical Allele Identifier: PA1139763044
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 894811
ClinVar RCV Id: RCV001136561 RCV001136562 RCV001136563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Asn56Asp
CA65850278
NM_025216.3:c.166A>G