Canonical Allele Identifier: PA645437266
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala1290Ser
CA6911463
NM_014363.6:c.3868G>T