Allele Registry

Canonical Allele Identifier: PA645461900

Gene: SLX4 HGNC NCBI

ClinVar Allele:

242430

ClinVar RCV:

RCV000234484

RCV000502872

RCV001084818

RCV001120033

RCV003939891

ClinVar Variation:

241698

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Val197Ala	CA7866815 NM_032444.4:c.590T>C