Canonical Allele Identifier: PA2825160475
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg39Pro
CA379966350
NM_000378.6:c.116G>C