Canonical Allele Identifier: PA2829999431
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930426
ClinVar RCV Id: RCV003789736
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr166Ser
CA379964872
NM_024424.5:c.497C>G
CA379964878
NM_024424.5:c.496A>T