Canonical Allele Identifier: PA2580354907
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2064730
ClinVar RCV Id: RCV002953643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile3680Thr
CA246651788
NM_014363.6:c.11039T>C