Canonical Allele Identifier: PA2825160948
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940962
ClinVar RCV Id: RCV003792224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys180Tyr
CA379964735
NM_000378.6:c.539G>A