Canonical Allele Identifier: PA658673630
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456321
ClinVar RCV Id: RCV000559513 RCV000764054 RCV003243177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Ile1423Val
CA276958396
NM_032444.4:c.4267A>G