Canonical Allele Identifier: PA891863849
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304422
ClinVar RCV Id: RCV000323122 RCV000347410 RCV000382270 RCV001521008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser232Thr
CA065489
NM_024426.6:c.695G>C