Canonical Allele Identifier: PA2825160461
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 645627
ClinVar RCV Id: RCV000799751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Val38Leu
CA379966359
NM_000378.6:c.112G>C