Canonical Allele Identifier: PA916075441
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 807722
ClinVar RCV Id: RCV000995915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly175Cys
CA379964782
NM_024426.6:c.523G>T