Canonical Allele Identifier: PA2830001110
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070809
ClinVar RCV Id: RCV004013319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Met74Val
CA379966132
NM_024426.6:c.220A>G