Canonical Allele Identifier: PA1139732451
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 938190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala4565Asp
CA6909932
NM_014363.6:c.13694C>A