Canonical Allele Identifier: PA645462080
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 262047
ClinVar RCV Id: RCV000245084 RCV000323962 RCV000515613 RCV001527973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Pro1122Leu
CA7865933
NM_032444.4:c.3365C>T