Canonical Allele Identifier: PA2830000707
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543128
ClinVar RCV Id: RCV000653791
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Met507Val
CA379957543
NM_024424.5:c.1519A>G