Canonical Allele Identifier: PA2829763909
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2727586
ClinVar RCV Id: RCV003588193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn1067Ser
CA6911554
NM_014363.6:c.3200A>G