Canonical Allele Identifier: PA1139750419
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 872897
ClinVar RCV Id: RCV001093599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Val167Asp
CA379964866
NM_024426.6:c.500T>A