Canonical Allele Identifier: PA2580461200
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445386
ClinVar RCV Id: RCV003154796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala154Val
CA379965013
NM_024426.6:c.461C>T