Canonical Allele Identifier: PA891863785
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543115
ClinVar RCV Id: RCV000653776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Leu58Val
CA379966233
NM_024426.6:c.172C>G