Canonical Allele Identifier: PA116262
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3489
ClinVar RCV Id: RCV000003660 RCV001376854
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Asp252Gly
CA016344
NM_001198551.1:c.755A>G