Allele Registry

Canonical Allele Identifier: PA645461994

Gene: SLX4 HGNC NCBI

ClinVar Variation Id: 414725

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Ala683Thr	CA7866305 NM_032444.4:c.2047G>A