Canonical Allele Identifier: PA2829763947
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2902901
ClinVar RCV Id: RCV003750768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Leu1131Val
CA6911532
NM_014363.6:c.3391C>G