Canonical Allele Identifier: PA916008676
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 802913
ClinVar RCV Id: RCV000988966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gly41Arg
CA6912057
NM_001278055.2:c.121G>A
CA387551958
NM_001278055.2:c.121G>C