Canonical Allele Identifier: PA645493869
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 423769
ClinVar RCV Id: RCV000483296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079492.2:p.Val81Ala
CA16617469
NM_025216.3:c.242T>C