Canonical Allele Identifier: PA2825160836
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421888
ClinVar RCV Id: RCV001923870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.His142Gln
CA379965681
NM_000378.6:c.426C>G
CA379965683
NM_000378.6:c.426C>A