Canonical Allele Identifier: PA2580354612
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2138947
ClinVar RCV Id: RCV003050759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile2337Val
CA6910980
NM_014363.6:c.7009A>G