Canonical Allele Identifier: PA2825160587
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 965500
ClinVar RCV Id: RCV001239966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro71Thr
CA379966154
NM_000378.6:c.211C>A