Canonical Allele Identifier: PA891863829
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438653
ClinVar RCV Id: RCV000505662 RCV001377140
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly171Val
CA379964820
NM_024426.6:c.512G>T