Canonical Allele Identifier: PA2825160893
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383500
ClinVar RCV Id: RCV001892642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Glu159Asp
CA379964949
NM_000378.6:c.477G>T
CA379964951
NM_000378.6:c.477G>C