Canonical Allele Identifier: PA891856069
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 582506
ClinVar RCV Id: RCV000706597 RCV001825402 RCV004544952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg69Trp
CA2113856
NM_025216.3:c.205C>T