Canonical Allele Identifier: PA645462073
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 319162
ClinVar RCV Id: RCV000351349 RCV000679857 RCV002223834 RCV001820946 RCV003391153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Gly992Glu
CA7866027
NM_032444.4:c.2975G>A