Canonical Allele Identifier: PA2829998851
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576484
ClinVar RCV Id: RCV000698991
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro41Ala
CA379966341
NM_024424.5:c.121C>G