Canonical Allele Identifier: PA2829998849
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_077742.3:p.Pro41Ser
CA219511447
NM_024424.5:c.121C>T