Canonical Allele Identifier: PA1139731255
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 982742
ClinVar RCV Id: RCV001262393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp2566Gly
CA387518446
NM_014363.6:c.7697A>G