Canonical Allele Identifier: PA2826578396
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2730538
ClinVar RCV Id: RCV003588313
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Thr3565Ile
CA6910336
NM_001278055.2:c.10694C>T