Canonical Allele Identifier: PA2573282929
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397701
ClinVar RCV Id: RCV001922394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro71Ser
CA379966152
NM_024426.6:c.211C>T