Canonical Allele Identifier: PA2825160777
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2921656
ClinVar RCV Id: RCV003782678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Pro127Leu
CA379965810
NM_000378.6:c.380C>T