Canonical Allele Identifier: PA2825160366
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala10Tyr
CA658797616
NM_000378.6:c.28_29delinsTA