Canonical Allele Identifier: PA2826577384
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 3157483
ClinVar RCV Id: RCV004447326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val2146Ala
CA246657627
NM_001278055.2:c.6437T>C