Canonical Allele Identifier: PA2829999320
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421888
ClinVar RCV Id: RCV001923870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.His142Gln
CA379965681
NM_024424.5:c.426C>G
CA379965683
NM_024424.5:c.426C>A