Canonical Allele Identifier: PA2825160455
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 971749
ClinVar RCV Id: RCV001247602

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly37Ala
CA379966361
NM_000378.6:c.110G>C