Canonical Allele Identifier: PA334514
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188281
ClinVar RCV Id: RCV000168266 RCV001121728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Ser1123Pro
CA334512
NM_032444.4:c.3367T>C