Canonical Allele Identifier: PA2830030993
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3190700
ClinVar RCV Id: RCV004483108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Leu67Pro
CA2113855
NM_025216.3:c.200T>C