Allele Registry

Canonical Allele Identifier: PA658673508

Gene: SLX4 HGNC NCBI

ClinVar Variation Id: 456339

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Arg278Gln	CA7866728 NM_032444.4:c.833G>A