Canonical Allele Identifier: PA2830002789
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_077744.4:p.Asp469Gly
CA016344
NM_024426.6:c.1406A>G