Canonical Allele Identifier: PA2830000758
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930682
ClinVar RCV Id: RCV003789992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Leu6Pro
CA379966565
NM_024426.6:c.17T>C