Canonical Allele Identifier: PA2826576192
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1033689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val396Met
CA6911882
NM_001278055.2:c.1186G>A