Canonical Allele Identifier: PA2580355122
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1703979
ClinVar RCV Id: RCV002281314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ser4407Asn
CA6910001
NM_014363.6:c.13220G>A