Canonical Allele Identifier: PA1139750295
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 836130
ClinVar RCV Id: RCV001037182 RCV004004708
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro137Ala
CA379965745
NM_024426.6:c.409C>G