Canonical Allele Identifier: PA2829998937
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543115
ClinVar RCV Id: RCV000653776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Leu58Val
CA379966233
NM_024424.5:c.172C>G