Canonical Allele Identifier: PA2825160460
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424959
ClinVar RCV Id: RCV001924167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Val38Phe
CA379966357
NM_000378.6:c.112G>T