Canonical Allele Identifier: PA2830002166
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Asn298Asp
CA379962216
NM_024426.6:c.892A>G