Canonical Allele Identifier: PA207203
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 212114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn1489Ser
CA207202
NM_014363.6:c.4466A>G