Canonical Allele Identifier: PA2826578155
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 882123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His3219Tyr
CA387512977
NM_001278055.2:c.9655C>T