Canonical Allele Identifier: PA2825160546
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721291
ClinVar RCV Id: RCV002294960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Leu58Arg
CA379966230
NM_000378.6:c.173T>G