Canonical Allele Identifier: PA2825160581
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 951676
ClinVar RCV Id: RCV001223644
ClinVar Variation Id: 1057250
ClinVar RCV Id: RCV001366196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly68Arg
CA379966172
NM_000378.6:c.202G>C
CA379966173
NM_000378.6:c.202G>A