Canonical Allele Identifier: PA658673507
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456338
ClinVar RCV Id: RCV000534649 RCV001290535 RCV001764528 RCV003237892
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Amino-acid Alleles

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