Canonical Allele Identifier: PA916075427
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 658496
ClinVar RCV Id: RCV000815329 RCV004001775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro127Arg
CA379965811
NM_024426.6:c.380C>G