Canonical Allele Identifier: PA2829998978
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397701
ClinVar RCV Id: RCV001922394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro71Ser
CA379966152
NM_024424.5:c.211C>T