Canonical Allele Identifier: PA658673596
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456315
ClinVar RCV Id: RCV000545382 RCV001821491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Pro1261Leu
CA7865834
NM_032444.4:c.3782C>T