Canonical Allele Identifier: PA2825160950
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2155887
ClinVar RCV Id: RCV003072564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg181Gly
CA379964726
NM_000378.6:c.541C>G