Canonical Allele Identifier: PA2826576742
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1343989
ClinVar RCV Id: RCV001847534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala1226Ser
CA387532419
NM_001278055.2:c.3676G>T