Canonical Allele Identifier: PA2825161547
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406697
ClinVar RCV Id: RCV000456332 RCV003322772 RCV003463880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Asn387Thr
CA064353
NM_000378.6:c.1160A>C