Canonical Allele Identifier: PA2825160914
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474384
ClinVar RCV Id: RCV002005490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala164Pro
CA379964899
NM_000378.6:c.490G>C