Canonical Allele Identifier: PA2826578144
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2902799
ClinVar RCV Id: RCV003750765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Glu3209Asp
CA6910514
NM_001278055.2:c.9627G>C
CA387513036
NM_001278055.2:c.9627G>T