Canonical Allele Identifier: PA2580354869
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2164138
ClinVar RCV Id: RCV003082025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile3466Met
CA6910457
NM_014363.6:c.10398T>G