Canonical Allele Identifier: PA2825160426
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926717
ClinVar RCV Id: RCV003788955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser25Pro
CA379966443
NM_000378.6:c.73T>C