Canonical Allele Identifier: PA2825160917
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930426
ClinVar RCV Id: RCV003789736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Thr166Ser
CA379964872
NM_000378.6:c.497C>G
CA379964878
NM_000378.6:c.496A>T