Canonical Allele Identifier: PA645461865
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414706
ClinVar RCV Id: RCV000472372 RCV001821331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Gly25Arg
CA7866959
NM_032444.4:c.73G>A
CA394548018
NM_032444.4:c.73G>C