Allele Registry

Canonical Allele Identifier: PA645462109

Gene: SLX4 HGNC NCBI

ClinVar Variation Id: 436780

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Ile1124Val	CA7865928 NM_032444.4:c.3370A>G