Canonical Allele Identifier: PA645462026
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407899
ClinVar RCV Id: RCV000463301 RCV001121834 RCV001796060 RCV001821253 RCV003902645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Glu769Gln
CA7866204
NM_032444.4:c.2305G>C