Canonical Allele Identifier: PA916002465
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Asn81Asp
CA379962216
NM_001198552.2:c.241A>G