Canonical Allele Identifier: PA2825161325
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662183
ClinVar RCV Id: RCV003443678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Tyr300His
CA065855
NM_000378.6:c.898T>C