Canonical Allele Identifier: PA2825160400
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1718400
ClinVar RCV Id: RCV002304892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala18Ser
CA379966487
NM_000378.6:c.52G>T