Allele Registry

Canonical Allele Identifier: PA658673647

Gene: SLX4 HGNC NCBI

ClinVar Variation Id: 456329

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Arg1589Cys	CA7865511 NM_032444.4:c.4765C>T