Canonical Allele Identifier: PA2826222878
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478819
ClinVar RCV Id: RCV001990786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.His147Asn
CA379960301
NM_001198551.1:c.439C>A
CA2573146220
NM_001198551.1:c.438_439delinsAA