Canonical Allele Identifier: PA2825160368
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057387
ClinVar RCV Id: RCV001366357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser11Cys
CA379966529
NM_000378.6:c.32C>G