Canonical Allele Identifier: PA2499290214
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057087
ClinVar RCV Id: RCV001366006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser123Leu
CA379965835
NM_024426.6:c.368C>T