Canonical Allele Identifier: PA658673641
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 456327
ClinVar RCV Id: RCV000540214 RCV000585421 RCV001121625
ClinVar Variation Id: 1938560
ClinVar RCV Id: RCV002646411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Met1530Ile
CA7865592
NM_032444.4:c.4590G>A
CA276958017
NM_032444.4:c.4590G>T
CA394516823
NM_032444.4:c.4590G>C