Canonical Allele Identifier: PA2825160742
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024394
ClinVar RCV Id: RCV001324569 RCV004005124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly117Asp
CA219511109
NM_000378.6:c.350G>A