Canonical Allele Identifier: PA645462037
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 241672
ClinVar RCV Id: RCV000234592 RCV000764059 RCV001194825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Ala870Val
CA7866124
NM_032444.4:c.2609C>T