Canonical Allele Identifier: PA2580354283
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2167360
ClinVar RCV Id: RCV003092102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn559Asp
CA387547267
NM_014363.6:c.1675A>G