Canonical Allele Identifier: PA2826578042
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1126212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val3074Met
CA6910587
NM_001278055.2:c.9220G>A