Canonical Allele Identifier: PA2830002186
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 78338
ClinVar RCV Id: RCV000735857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser304Phe
CA219496211
NM_024426.6:c.911C>T