Canonical Allele Identifier: PA2825161721
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476690
ClinVar RCV Id: RCV000538982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.His488Gln
CA379957558
NM_000378.6:c.1464C>A
CA379957559
NM_000378.6:c.1464C>G