Canonical Allele Identifier: PA2825160362
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala10Asp
CA379966534
NM_000378.6:c.29C>A