Canonical Allele Identifier: PA645461958
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407935
ClinVar RCV Id: RCV000519850 RCV000764064 RCV001088147 RCV001194850 RCV003492056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Lys458Glu
CA7866534
NM_032444.4:c.1372A>G