Canonical Allele Identifier: PA2580470814
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2056394
ClinVar RCV Id: RCV002938535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Cys416Ser
CA350592859
NM_025216.3:c.1246T>A
CA350592886
NM_025216.3:c.1247G>C