Canonical Allele Identifier: PA645493890
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334399
ClinVar RCV Id: RCV000283655 RCV000346906 RCV000845116 RCV000521785 RCV004530358 RCV000406139 RCV001083663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Gly165Arg
CA2113950
NM_025216.3:c.493G>A
CA350585818
NM_025216.3:c.493G>C