Canonical Allele Identifier: PA2825160380
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406699
ClinVar RCV Id: RCV000457233
ClinVar Variation Id: 1512513
ClinVar RCV Id: RCV002023068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr12Pro
CA064742
NM_000378.6:c.34A>C
CA2573146221
NM_000378.6:c.33_34delinsAC