Canonical Allele Identifier: PA2825160721
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948439
ClinVar RCV Id: RCV003809213
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Phe113Ser
CA379965895
NM_000378.6:c.338T>C