Canonical Allele Identifier: PA2741986819
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2947644
ClinVar RCV Id: RCV003804274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro130Leu
CA379965796
NM_024426.6:c.389C>T