Canonical Allele Identifier: PA2825160740
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679630
ClinVar RCV Id: RCV003464887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly117Ser
CA379965874
NM_000378.6:c.349G>A