Canonical Allele Identifier: PA1139730903
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 882478
ClinVar RCV Id: RCV001112182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Leu2024Val
CA6911142
NM_014363.6:c.6070C>G