Canonical Allele Identifier: PA2829998696
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063197
ClinVar RCV Id: RCV001373013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro15Leu
CA379966504
NM_024424.5:c.44C>T