Canonical Allele Identifier: PA2825160702
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476699
ClinVar RCV Id: RCV000545211 RCV000709150 RCV000763735 RCV001568364 RCV003139859 RCV003459256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala105Gly
CA219511175
NM_000378.6:c.314C>G