Allele Registry

Canonical Allele Identifier: PA2825160929

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000505662

RCV001377140

ClinVar Variation:

438653

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Gly171Val	CA379964820 NM_000378.6:c.512G>T