Canonical Allele Identifier: PA2826578212
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1463230
ClinVar RCV Id: RCV001960942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3300Leu
CA387512425
NM_001278055.2:c.9899C>T