Allele Registry

Canonical Allele Identifier: PA645462184

Gene: SLX4 HGNC NCBI

ClinVar Variation Id: 436779

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Ser1342Gly	CA7865760 NM_032444.4:c.4024A>G