Canonical Allele Identifier: PA2829999188
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2952202
ClinVar RCV Id: RCV003815353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser119Leu
CA379965860
NM_024424.5:c.356C>T