Canonical Allele Identifier: PA2830000854
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073049
ClinVar RCV Id: RCV004015063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Thr22Lys
CA379966458
NM_024426.6:c.65C>A