Canonical Allele Identifier: PA2826578306
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 805282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Met3432Ile
CA6910403
NM_001278055.2:c.10296G>A
CA6910404
NM_001278055.2:c.10296G>T
CA387511531
NM_001278055.2:c.10296G>C