Canonical Allele Identifier: PA891863777
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576484
ClinVar RCV Id: RCV000698991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro41Ala
CA379966341
NM_024426.6:c.121C>G