Canonical Allele Identifier: PA645461988
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 319169
ClinVar RCV Id: RCV000386591 RCV000500030 RCV001094239 RCV003409497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg669His
CA7866337
NM_032444.4:c.2006G>A