Canonical Allele Identifier: PA645461866
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407911
ClinVar RCV Id: RCV000473920 RCV001118600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Arg29His
CA7866955
NM_032444.4:c.86G>A