Canonical Allele Identifier: PA2825160444
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2950348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln31Glu
CA219511455
NM_000378.6:c.91C>G