Canonical Allele Identifier: PA645461883
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 423992
ClinVar RCV Id: RCV000478235 RCV000766462 RCV001087098 RCV001120334 RCV003902732
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Gly141Val
CA7866879
NM_032444.4:c.422G>T