Canonical Allele Identifier: PA2830002016
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180586
ClinVar RCV Id: RCV000157583 RCV000892804 RCV003162657 RCV002492615 RCV004551354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Met255Lys
CA016452
NM_024426.6:c.764T>A