Canonical Allele Identifier: PA1139749812
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 944939
ClinVar RCV Id: RCV001215452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala50Asp
CA219511376
NM_024426.6:c.149C>A