Canonical Allele Identifier: PA645462046
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407922
ClinVar RCV Id: RCV000471089 RCV001821256 RCV002221540 RCV002525559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Thr919Ile
CA7866078
NM_032444.4:c.2756C>T