Canonical Allele Identifier: PA916075379
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 654910
ClinVar RCV Id: RCV000810979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Val78Met
CA379966106
NM_024426.6:c.232G>A