Canonical Allele Identifier: PA1139749867
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 951676
ClinVar RCV Id: RCV001223644
ClinVar Variation Id: 1057250
ClinVar RCV Id: RCV001366196
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly68Arg
CA379966172
NM_024426.6:c.202G>C
CA379966173
NM_024426.6:c.202G>A