Canonical Allele Identifier: PA2826578033
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2573663
ClinVar RCV Id: RCV003317999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3065Phe
CA387513992
NM_001278055.2:c.9194C>T