Canonical Allele Identifier: PA658808633
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 522555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn2860Ser
CA6910745
NM_014363.6:c.8579A>G