Canonical Allele Identifier: PA2825160516
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069615
ClinVar RCV Id: RCV004008159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gly49Ser
CA379966289
NM_000378.6:c.145G>A