Canonical Allele Identifier: PA2826576696
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala1143Ser
CA6911463
NM_001278055.2:c.3427G>T