Canonical Allele Identifier: PA2580354585
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2071467
ClinVar RCV Id: RCV002975603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn2141Ser
CA387521911
NM_014363.6:c.6422A>G