Canonical Allele Identifier: PA2830000763
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2155557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Leu6Gly
CA2580084217
NM_024426.6:c.16_17delinsGG