Canonical Allele Identifier: PA1139731923
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 968056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His3480Tyr
CA6910453
NM_014363.6:c.10438C>T