Canonical Allele Identifier: PA2825160503
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009526
ClinVar RCV Id: RCV001307032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly43Cys
CA379966330
NM_000378.6:c.127G>T