Canonical Allele Identifier: PA2829999443
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404984
ClinVar RCV Id: RCV001899146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Phe169Leu
CA379964839
NM_024424.5:c.507T>G
CA379964841
NM_024424.5:c.507T>A
CA379964848
NM_024424.5:c.505T>C