Canonical Allele Identifier: PA2825160532
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2093007
ClinVar RCV Id: RCV003008350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Ser54Thr
CA379966255
NM_000378.6:c.161G>C