Canonical Allele Identifier: PA891863886
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543128
ClinVar RCV Id: RCV000653791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Met510Val
CA379957543
NM_024426.6:c.1528A>G