Allele Registry

Canonical Allele Identifier: PA2741986850

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 2935359

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Phe173Leu	CA379964795 NM_024426.6:c.519C>G CA379964796 NM_024426.6:c.519C>A CA379964804 NM_024426.6:c.517T>C