Canonical Allele Identifier: PA2826578253
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2316774
ClinVar RCV Id: RCV002919608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3359Arg
CA387512033
NM_001278055.2:c.10077T>G
CA387512034
NM_001278055.2:c.10077T>A
CA387512040
NM_001278055.2:c.10075A>C