Canonical Allele Identifier: PA645462016
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414707
ClinVar RCV Id: RCV000468690 RCV001821332 RCV002489115 RCV003441891 RCV003915301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Glu701Asp
CA7866291
NM_032444.4:c.2103G>C
CA394526092
NM_032444.4:c.2103G>T