Canonical Allele Identifier: PA2830002049
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406688
ClinVar RCV Id: RCV000469273 RCV001107288 RCV001107289 RCV001107939 RCV002256254 RCV003313070 RCV004551518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly262Asp
CA065639
NM_024426.6:c.785G>A