Canonical Allele Identifier: PA2829999236
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2921656
ClinVar RCV Id: RCV003782678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Pro127Leu
CA379965810
NM_024424.5:c.380C>T