Canonical Allele Identifier: PA2499290192
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1176566
ClinVar RCV Id: RCV001532158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala164Val
CA379964895
NM_024426.6:c.491C>T