Canonical Allele Identifier: PA658831537
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 559186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Gly1169Ala
CA387534851
NM_014363.6:c.3506G>C