Canonical Allele Identifier: PA2825160504
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722064
ClinVar RCV Id: RCV002302341
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly43Arg
CA379966331
NM_000378.6:c.127G>C