Canonical Allele Identifier: PA2826576615
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala1035Val
CA6911512
NM_001278055.2:c.3104C>T