Canonical Allele Identifier: PA2825160786
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2947644
ClinVar RCV Id: RCV003804274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro130Leu
CA379965796
NM_000378.6:c.389C>T