Canonical Allele Identifier: PA2825160749
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543139
ClinVar RCV Id: RCV000653802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser119Pro
CA379965864
NM_000378.6:c.355T>C