Canonical Allele Identifier: PA208151
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 212221
ClinVar RCV Id: RCV000194162 RCV000204168 RCV000442623 RCV001094281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg1761Cys
CA208149
NM_032444.4:c.5281C>T