Canonical Allele Identifier: PA2825160499
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920843
ClinVar RCV Id: RCV002621182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly43Val
CA379966327
NM_000378.6:c.128G>T