Canonical Allele Identifier: PA2825160727
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ala114Val
CA379965888
NM_000378.6:c.341C>T