Canonical Allele Identifier: PA2825160907
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365771
ClinVar RCV Id: RCV001929946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser163Asn
CA379964906
NM_000378.6:c.488G>A