Canonical Allele Identifier: PA2580354613
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146373
ClinVar RCV Id: RCV003074528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp2339Gly
CA6910979
NM_014363.6:c.7016A>G