Canonical Allele Identifier: PA2825160844
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1980328
ClinVar RCV Id: RCV002761250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Phe144del
CA598508257
NM_000378.6:c.430_432del