Canonical Allele Identifier: PA2499290174
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063197
ClinVar RCV Id: RCV001373013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro15Leu
CA379966504
NM_024426.6:c.44C>T