Canonical Allele Identifier: PA916075414
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 654983
ClinVar RCV Id: RCV000811058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala114Glu
CA379965886
NM_024426.6:c.341C>A