Canonical Allele Identifier: PA2826576738
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2076536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro1225Thr
CA6911433
NM_001278055.2:c.3673C>A