Canonical Allele Identifier: PA2825160453
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940785
ClinVar RCV Id: RCV003800095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly37Glu
CA379966362
NM_000378.6:c.110G>A