Canonical Allele Identifier: PA1139750308
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 848604
ClinVar RCV Id: RCV001052395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro138Arg
CA379965734
NM_024426.6:c.413C>G