Canonical Allele Identifier: PA2825160768
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058424
ClinVar RCV Id: RCV001367563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly126Ala
CA379965818
NM_000378.6:c.377G>C