Canonical Allele Identifier: PA645437299
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Thr1741Ile
CA6911277
NM_014363.6:c.5222C>T