Canonical Allele Identifier: PA2825160933
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437098
ClinVar RCV Id: RCV001946529
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr174Ala
CA379964793
NM_000378.6:c.520A>G