Canonical Allele Identifier: PA2825160633
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 715223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala87Thr
CA064789
NM_000378.6:c.259G>A