Canonical Allele Identifier: PA2826577242
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2892958
ClinVar RCV Id: RCV003750599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu1929Val
CA6911115
NM_001278055.2:c.5785T>G