Canonical Allele Identifier: PA2825160446
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2945795
ClinVar RCV Id: RCV003803889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro33Gln
CA379966391
NM_000378.6:c.98C>A