Canonical Allele Identifier: PA2825160953
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg181Ser
CA379964728
NM_000378.6:c.541C>A