Canonical Allele Identifier: PA2826222669
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_001185480.1:p.Gly105Arg
CA379961993
NM_001198551.1:c.313G>C
CA379961994
NM_001198551.1:c.313G>A