Canonical Allele Identifier: PA891863787
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543142
ClinVar RCV Id: RCV000653805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser67Phe
CA379966174
NM_024426.6:c.200C>T