Canonical Allele Identifier: PA645462078
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414700
ClinVar RCV Id: RCV000461671 RCV000504053 RCV001116863 RCV003418213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg1060Trp
CA7865977
NM_032444.4:c.3178C>T