Canonical Allele Identifier: PA2741945016
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2917408
ClinVar RCV Id: RCV003751541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Glu2048Gly
CA6911128
NM_014363.6:c.6143A>G