Canonical Allele Identifier: PA658673591
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456313
ClinVar RCV Id: RCV000552069 RCV001572565 RCV001293953 RCV003151083 RCV003960260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg1226Trp
CA7865871
NM_032444.4:c.3676C>T