Canonical Allele Identifier: PA645461900
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 241698
ClinVar RCV Id: RCV000234484 RCV000502872 RCV001120033 RCV001084818 RCV003939891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Val197Ala
CA7866815
NM_032444.4:c.590T>C