Canonical Allele Identifier: PA1139749764
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861779
ClinVar RCV Id: RCV001068367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Asp40His
CA379966348
NM_024426.6:c.118G>C