Allele Registry

Canonical Allele Identifier: PA658673507

Gene: SLX4 HGNC NCBI

ClinVar Allele:

466440

ClinVar RCV:

RCV000534649

RCV001290535

RCV001764528

RCV003237892

ClinVar Variation:

456338

HGVS (amino-acid)	Matching Registered Transcripts
NP_115820.2:p.Arg278Trp	CA7866729 NM_032444.4:c.832C>T