Canonical Allele Identifier: PA2741919365
Gene: WNT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2854458
ClinVar RCV Id: RCV003688668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005421.1:p.Cys360Phe
CA384639171
NM_005430.4:c.1079G>T