Canonical Allele Identifier: PA658810907
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Asn81Asp
CA379962216
NM_001198551.1:c.241A>G