Canonical Allele Identifier: PA2825160900
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386369
ClinVar RCV Id: RCV001875288
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Cys161Phe
CA379964926
NM_000378.6:c.482G>T