Canonical Allele Identifier: PA2825160480
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2942653
ClinVar RCV Id: RCV003807819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Asp40Ala
CA379966346
NM_000378.6:c.119A>C