Canonical Allele Identifier: PA2825160930
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2938948
ClinVar RCV Id: RCV003791674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly171Arg
CA379964828
NM_000378.6:c.511G>C