Canonical Allele Identifier: PA2830000040
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3499
ClinVar RCV Id: RCV000003673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser346Gly
CA016356
NM_024424.5:c.1036A>G