Canonical Allele Identifier: PA2829998875
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630917
ClinVar RCV Id: RCV004550671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly49Arg
CA379966288
NM_024424.5:c.145G>C