Canonical Allele Identifier: PA2828276068
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543128
ClinVar RCV Id: RCV000653791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.Met114Val
CA379957543
NM_001367854.1:c.340A>G