Canonical Allele Identifier: PA645492388
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391706
ClinVar RCV Id: RCV000419959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Trp351Gly
CA16607302
NM_005430.4:c.1051T>G