Canonical Allele Identifier: PA645493867
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334394
ClinVar RCV Id: RCV000308592 RCV000401069 RCV000639740 RCV001545215 RCV000358786 RCV004530357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Arg70Trp
CA2113858
NM_025216.3:c.208C>T