Canonical Allele Identifier: PA891863778
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476676
ClinVar RCV Id: RCV000553840 RCV003318595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro41Ser
CA219511447
NM_024426.6:c.121C>T