Canonical Allele Identifier: PA354527
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 218673
ClinVar RCV Id: RCV000202661 RCV000893654 RCV002277561 RCV002494517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Ser88Arg
CA248864
NM_005430.4:c.264T>A
CA236608327
NM_005430.4:c.262A>C
CA384627948
NM_005430.4:c.264T>G