Canonical Allele Identifier: PA1139729895
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 949829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Tyr159His
CA387552158
NM_014363.6:c.475T>C