Canonical Allele Identifier: PA2826577290
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 837856
ClinVar RCV Id: RCV001039285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala2007Ser
CA387521747
NM_001278055.2:c.6019G>T