Canonical Allele Identifier: PA913197354
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 627583
ClinVar RCV Id: RCV000770974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Cys330Tyr
CA384637990
NM_005430.4:c.989G>A