Canonical Allele Identifier: PA891856075
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 569972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala2367Val
CA6910971
NM_014363.6:c.7100C>T