Canonical Allele Identifier: PA055999
Gene: WDR73 HGNC NCBI

Linked Data

ClinVar Variation Id: 242543
ClinVar RCV Id: RCV000785981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116245.2:p.Leu98Pro
CA055994
NM_032856.5:c.293T>C