Canonical Allele Identifier: PA2741986847
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2949798
ClinVar RCV Id: RCV003804964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Phe169Ser
CA379964844
NM_024426.6:c.506T>C