Canonical Allele Identifier: PA2826576213
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1492688
ClinVar RCV Id: RCV001981151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile418Leu
CA387547176
NM_001278055.2:c.1252A>C