Canonical Allele Identifier: PA2825160821
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2148870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro138Leu
CA379965733
NM_000378.6:c.413C>T