Canonical Allele Identifier: PA658673494
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456340
ClinVar RCV Id: RCV000527683 RCV001118601 RCV001821493 RCV001775845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg29Cys
CA7866957
NM_032444.4:c.85C>T