Canonical Allele Identifier: PA2825160929
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly171Val
CA379964820
NM_000378.6:c.512G>T