Canonical Allele Identifier: PA2829999403
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 579939
ClinVar RCV Id: RCV000703344 RCV002249420 RCV003999741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gln160His
CA379964936
NM_024424.5:c.480G>T
CA379964937
NM_024424.5:c.480G>C