Canonical Allele Identifier: PA2825160605
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3026662
ClinVar RCV Id: RCV003887055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Val78Leu
CA379966104
NM_000378.6:c.232G>T
CA379966105
NM_000378.6:c.232G>C