Canonical Allele Identifier: PA2825160561
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser63Arg
CA379966197
NM_000378.6:c.189C>G
CA379966198
NM_000378.6:c.189C>A
CA379966202
NM_000378.6:c.187A>C