Canonical Allele Identifier: PA2825160526
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1686385
ClinVar RCV Id: RCV002246898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Glu52Asp
CA379966266
NM_000378.6:c.156G>T
CA379966267
NM_000378.6:c.156G>C