Canonical Allele Identifier: PA658664557
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448203
ClinVar RCV Id: RCV000517093 RCV001834669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn1138Ser
CA387535393
NM_014363.6:c.3413A>G