Canonical Allele Identifier: PA2830000818
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2418325
ClinVar RCV Id: RCV003121074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Val14Leu
CA379966514
NM_024426.6:c.40G>C