Canonical Allele Identifier: PA2830002214
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948230
ClinVar RCV Id: RCV003807052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly322Arg
CA379961993
NM_024426.6:c.964G>C
CA379961994
NM_024426.6:c.964G>A