Canonical Allele Identifier: PA2829998665
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 802670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala10Ser
CA379966536
NM_024424.5:c.28G>T