Canonical Allele Identifier: PA2830001065
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072645
ClinVar RCV Id: RCV004013667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg64Leu
CA379966191
NM_024426.6:c.191G>T