Canonical Allele Identifier: PA2741986769
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2925823
ClinVar RCV Id: RCV003783917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg61Gln
CA379966214
NM_024426.6:c.182G>A