Canonical Allele Identifier: PA2825160457
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly37Arg
CA379966364
NM_000378.6:c.109G>C
CA379966365
NM_000378.6:c.109G>A