Canonical Allele Identifier: PA916075483
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3499
ClinVar RCV Id: RCV000003673
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser346Gly
CA016356
NM_024426.6:c.1036A>G