Canonical Allele Identifier: PA2825161366
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948230
ClinVar RCV Id: RCV003807052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly322Ser
CA379961994
NM_000378.6:c.964G>A