Canonical Allele Identifier: PA2826577760
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1957054
ClinVar RCV Id: RCV002706008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gly2666Arg
CA246654262
NM_001278055.2:c.7996G>A
CA387516637
NM_001278055.2:c.7996G>C