Canonical Allele Identifier: PA2825160397
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2936526
ClinVar RCV Id: RCV003798764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala18Glu
CA379966486
NM_000378.6:c.53C>A