Canonical Allele Identifier: PA2825160731
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 570963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro115His
CA379965883
NM_000378.6:c.344C>A