Canonical Allele Identifier: PA2825160398
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 656347
ClinVar RCV Id: RCV000812742 RCV001258177
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala18Pro
CA379966489
NM_000378.6:c.52G>C