Canonical Allele Identifier: PA116294
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3499
ClinVar RCV Id: RCV000003673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Ser129Gly
CA016356
NM_001198551.1:c.385A>G