Canonical Allele Identifier: PA1139749717
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839433
ClinVar RCV Id: RCV001041189
ClinVar Variation Id: 1055328
ClinVar RCV Id: RCV001363977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly26Arg
CA379966437
NM_024426.6:c.76G>C
CA379966438
NM_024426.6:c.76G>A