Canonical Allele Identifier: PA2825160535
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1524014
ClinVar RCV Id: RCV002031406
ClinVar Variation Id: 2241588
ClinVar RCV Id: RCV002747564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala55Val
CA219511362
NM_000378.6:c.164C>T
CA2573146210
NM_000378.6:c.164_165delinsTG