Canonical Allele Identifier: PA2826578222
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2164138
ClinVar RCV Id: RCV003082025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile3319Met
CA6910457
NM_001278055.2:c.9957T>G