Canonical Allele Identifier: PA2825160431
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839433
ClinVar RCV Id: RCV001041189
ClinVar Variation Id: 1055328
ClinVar RCV Id: RCV001363977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly26Arg
CA379966437
NM_000378.6:c.76G>C
CA379966438
NM_000378.6:c.76G>A