Canonical Allele Identifier: PA891863830
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584761
ClinVar RCV Id: RCV000709145 RCV001295549
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg181Ser
CA379964728
NM_024426.6:c.541C>A