Canonical Allele Identifier: PA2826576165
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg368Cys
CA6911901
NM_001278055.2:c.1102C>T