Canonical Allele Identifier: PA2580354758
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2316775
ClinVar RCV Id: RCV002897587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Phe3026Ile
CA387515243
NM_014363.6:c.9076T>A