Canonical Allele Identifier: PA2826576869
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 989207
ClinVar RCV Id: RCV001391619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg1428Pro
CA387527940
NM_001278055.2:c.4283G>C