Canonical Allele Identifier: PA1139750363
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 941538
ClinVar RCV Id: RCV001211333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Glu155Lys
CA379965008
NM_024426.6:c.463G>A