Canonical Allele Identifier: PA2580354614
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2082858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn2351Ser
CA387520154
NM_014363.6:c.7052A>G