Canonical Allele Identifier: PA645462313
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 241697
ClinVar RCV Id: RCV000243677 RCV000440447 RCV001121536 RCV001086807
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Asn1834Ser
CA7865286
NM_032444.4:c.5501A>G