Canonical Allele Identifier: PA2829998819
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 971749
ClinVar RCV Id: RCV001247602
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly37Ala
CA379966361
NM_024424.5:c.110G>C