Canonical Allele Identifier: PA2829998863
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009526
ClinVar RCV Id: RCV001307032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly43Cys
CA379966330
NM_024424.5:c.127G>T