Canonical Allele Identifier: PA2825160404
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 955292
ClinVar RCV Id: RCV001227903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.His21Leu
CA379966464
NM_000378.6:c.62A>T