Canonical Allele Identifier: PA658664617
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 458269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile2146Val
CA387521847
NM_014363.6:c.6436A>G