Canonical Allele Identifier: PA2829998973
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474295
ClinVar RCV Id: RCV002005473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Glu70Asp
CA064727
NM_024424.5:c.210G>T
CA379966155
NM_024424.5:c.210G>C