Canonical Allele Identifier: PA916047019
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_001354783.1:p.Asp73Gly
CA016344
NM_001367854.1:c.218A>G