Canonical Allele Identifier: PA2826577848
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 884077
ClinVar RCV Id: RCV001114946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys2806Thr
CA387515713
NM_001278055.2:c.8417A>C