Canonical Allele Identifier: PA645493877
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 372548
ClinVar RCV Id: RCV000413047 RCV000991159 RCV001080960 RCV004530509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg113Cys
CA501169
NM_025216.3:c.337C>T