Canonical Allele Identifier: PA2825160586
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397701
ClinVar RCV Id: RCV001922394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro71Ser
CA379966152
NM_000378.6:c.211C>T