Canonical Allele Identifier: PA2826578180
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 648020
ClinVar RCV Id: RCV000802657 RCV001274921 RCV001662833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp3255Gly
CA6910487
NM_001278055.2:c.9764A>G