Canonical Allele Identifier: PA2580354870
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1929660
ClinVar RCV Id: RCV002626401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile3485Thr
CA6910449
NM_014363.6:c.10454T>C