Canonical Allele Identifier: PA2825160422
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Arg24Gly
CA379966448
NM_000378.6:c.70C>G