Canonical Allele Identifier: PA2580354482
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2020005
ClinVar RCV Id: RCV002852244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Lys1755Glu
CA6911273
NM_014363.6:c.5263A>G