Canonical Allele Identifier: PA2825160391
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071228
ClinVar RCV Id: RCV004014730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro17Thr
CA379966495
NM_000378.6:c.49C>A