Canonical Allele Identifier: PA645462219
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 241691
ClinVar RCV Id: RCV000231368 RCV001116752 RCV001194856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Thr1476Ser
CA7865641
NM_032444.4:c.4427C>G
CA394517166
NM_032444.4:c.4426A>T