Canonical Allele Identifier: PA2829999358
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011095
ClinVar RCV Id: RCV001308847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser150Asn
CA379965063
NM_024424.5:c.449G>A