Canonical Allele Identifier: PA2825160507
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Trp45Gly
CA379966317
NM_000378.6:c.133T>G