Canonical Allele Identifier: PA2825160364
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 802670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala10Ser
CA379966536
NM_000378.6:c.28G>T