Canonical Allele Identifier: PA1139749690
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 955292
ClinVar RCV Id: RCV001227903
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.His21Leu
CA379966464
NM_024426.6:c.62A>T