Canonical Allele Identifier: PA2826222621
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2934796
ClinVar RCV Id: RCV003798498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Ser87Pro
CA379962174
NM_001198551.1:c.259T>C