Canonical Allele Identifier: PA2580354279
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1950069
ClinVar RCV Id: RCV002671445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Val548Ala
CA6911877
NM_014363.6:c.1643T>C