Canonical Allele Identifier: PA2825160604
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 858711
ClinVar RCV Id: RCV001064647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Asp77Glu
CA379966107
NM_000378.6:c.231C>G
CA379966108
NM_000378.6:c.231C>A