Canonical Allele Identifier: PA2830000768
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072299
ClinVar RCV Id: RCV004012329
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro9Ala
CA379966542
NM_024426.6:c.25C>G