Canonical Allele Identifier: PA2825160769
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1981784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly126Arg
CA379965820
NM_000378.6:c.376G>C