Canonical Allele Identifier: PA162812
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135453
ClinVar RCV Id: RCV000122310 RCV001107941 RCV001107942 RCV000782221 RCV001081231 RCV001107940 RCV002255305 RCV002284191 RCV004551194 RCV003588578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Pro37Ser
CA016444
NM_001198551.1:c.109C>T