Canonical Allele Identifier: PA2825160855
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 937264
ClinVar RCV Id: RCV001206237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro149Gln
CA379965073
NM_000378.6:c.446C>A