Canonical Allele Identifier: PA891863802
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522546
ClinVar RCV Id: RCV000625689 RCV001860465
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala114Val
CA379965888
NM_024426.6:c.341C>T