Canonical Allele Identifier: PA2825160421
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839396
ClinVar RCV Id: RCV001041139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg24His
CA379966447
NM_000378.6:c.71G>A