Canonical Allele Identifier: PA2741919361
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2692186
ClinVar RCV Id: RCV003494383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Cys353Trp
CA384639014
NM_005430.4:c.1059C>G