Canonical Allele Identifier: PA2829999450
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2935359
ClinVar RCV Id: RCV003791013
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Phe173Leu
CA379964795
NM_024424.5:c.519C>G
CA379964796
NM_024424.5:c.519C>A
CA379964804
NM_024424.5:c.517T>C