Canonical Allele Identifier: PA2825161357
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620630
ClinVar RCV Id: RCV000761158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly317Glu
CA379962044
NM_000378.6:c.950G>A