Canonical Allele Identifier: PA2829998738
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1434182
ClinVar RCV Id: RCV001984564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.His21Arg
CA379966465
NM_024424.5:c.62A>G