Allele Registry

Canonical Allele Identifier: PA891863837

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000475587

RCV002746126

ClinVar Variation:

406694

1972352

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Asn203Lys	CA16613601 NM_024426.6:c.609C>G CA379964538 NM_024426.6:c.609C>A