Canonical Allele Identifier: PA2826575927
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 949829
ClinVar RCV Id: RCV001221388 RCV001836169 RCV003294062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Tyr12His
CA387552158
NM_001278055.2:c.34T>C