Canonical Allele Identifier: PA2829999957
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948230
ClinVar RCV Id: RCV003807052
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly322Arg
CA379961993
NM_024424.5:c.964G>C
CA379961994
NM_024424.5:c.964G>A