Canonical Allele Identifier: PA2829998825
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 645627
ClinVar RCV Id: RCV000799751
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val38Leu
CA379966359
NM_024424.5:c.112G>C