Canonical Allele Identifier: PA2825160352
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948393
ClinVar RCV Id: RCV003807215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Asp8Val
CA379966546
NM_000378.6:c.23A>T