Canonical Allele Identifier: PA2580461218
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Val167Ala
CA379964865
NM_024426.6:c.500T>C