Canonical Allele Identifier: PA2825160902
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930097
ClinVar RCV Id: RCV003787455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys161Gly
CA379964931
NM_000378.6:c.481T>G