Allele Registry

Canonical Allele Identifier: PA645461938

Gene: SLX4 HGNC NCBI

ClinVar RCV:

RCV000461785

ClinVar Variation:

407921

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Thr325Ser	CA7866665 NM_032444.4:c.973A>T