Canonical Allele Identifier: PA2580354582
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2138129
ClinVar RCV Id: RCV003064501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala2121Val
CA387522157
NM_014363.6:c.6362C>T