Canonical Allele Identifier: PA891856073
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 575490
ClinVar RCV Id: RCV000697721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Gln71Leu
CA2113861
NM_025216.3:c.212A>T