Canonical Allele Identifier: PA645461973
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 414709
ClinVar RCV Id: RCV000480800 RCV001085760 RCV000767083 RCV000989501 RCV001731703
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Tyr546Cys
CA7866469
NM_032444.4:c.1637A>G