Canonical Allele Identifier: PA2825160772
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1434347
ClinVar RCV Id: RCV001952868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly126Cys
CA379965819
NM_000378.6:c.376G>T