Canonical Allele Identifier: PA891863852
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_077744.4:p.Gly326Ala
CA5934315
NM_024426.6:c.977G>C
CA2579961810
NM_024426.6:c.977_978delinsCT
CA2579961811
NM_024426.6:c.977_978delinsCC
CA2579961813
NM_024426.6:c.977_978delinsCA