Canonical Allele Identifier: PA2825160935
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 939598
ClinVar RCV Id: RCV001209022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly175Asp
CA379964781
NM_000378.6:c.524G>A