Canonical Allele Identifier: PA2829998719
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071228
ClinVar RCV Id: RCV004014730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro17Thr
CA379966495
NM_024424.5:c.49C>A