Canonical Allele Identifier: PA658666013
Gene: WNT10B HGNC NCBI

Linked Data

ClinVar Variation Id: 452097
ClinVar RCV Id: RCV000520692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003385.2:p.Arg363Gly
CA384671277
NM_003394.3:c.1087C>G