Canonical Allele Identifier: PA2825160939
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679631
ClinVar RCV Id: RCV003464888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala177Asp
CA379964762
NM_000378.6:c.530C>A