Canonical Allele Identifier: PA645462081
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 436793
ClinVar RCV Id: RCV000501939 RCV000539205 RCV001764495 RCV003237884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Ser1123Tyr
CA7865930
NM_032444.4:c.3368C>A