Canonical Allele Identifier: PA2825160778
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 658496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro127Arg
CA379965811
NM_000378.6:c.380C>G