Canonical Allele Identifier: PA093214
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 4462
ClinVar RCV Id: RCV000004717 RCV000255788 RCV000550721 RCV000445356 RCV000622932 RCV000754840 RCV000845113 RCV001535660 RCV001729336 RCV001813948 RCV002227016 RCV004528071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Phe228Ile
CA116867
NM_025216.3:c.682T>A