Canonical Allele Identifier: PA2829999900
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543137
ClinVar RCV Id: RCV000653800 RCV003465415
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Asn298Asp
CA379962216
NM_024424.5:c.892A>G