Canonical Allele Identifier: PA645462028
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407938
ClinVar RCV Id: RCV000464063 RCV000502866 RCV001121832 RCV001081719 RCV003912802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Glu787Lys
CA7866169
NM_032444.4:c.2359G>A