Canonical Allele Identifier: PA2826578736
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 3157472
ClinVar RCV Id: RCV004447315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Thr4020Ala
CA6910140
NM_001278055.2:c.12058A>G