Canonical Allele Identifier: PA916047003
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406697
ClinVar RCV Id: RCV000456332 RCV003322772 RCV003463880
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Asn8Thr
CA064353
NM_001367854.1:c.23A>C