Canonical Allele Identifier: PA2826576503
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 458262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His804Gln
CA6911606
NM_001278055.2:c.2412C>A
CA387537475
NM_001278055.2:c.2412C>G