Canonical Allele Identifier: PA2829998954
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072645
ClinVar RCV Id: RCV004013667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg64Leu
CA379966191
NM_024424.5:c.191G>T