Canonical Allele Identifier: PA2741986850
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2935359
ClinVar RCV Id: RCV003791013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Phe173Leu
CA379964795
NM_024426.6:c.519C>G
CA379964796
NM_024426.6:c.519C>A
CA379964804
NM_024426.6:c.517T>C