Canonical Allele Identifier: PA2830000699
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476690
ClinVar RCV Id: RCV000538982
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.His505Gln
CA379957558
NM_024424.5:c.1515C>A
CA379957559
NM_024424.5:c.1515C>G