Canonical Allele Identifier: PA2826222680
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403610
ClinVar RCV Id: RCV000454436 RCV000695577 RCV001029773 RCV004000608 RCV002510892 RCV003463834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Gly109Ala
CA5934315
NM_001198551.1:c.326G>C
CA2579961810
NM_001198551.1:c.326_327delinsCT
CA2579961811
NM_001198551.1:c.326_327delinsCC
CA2579961813
NM_001198551.1:c.326_327delinsCA