Canonical Allele Identifier: PA2826579008
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 554337
ClinVar RCV Id: RCV000669953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn4402Asp
CA387504800
NM_001278055.2:c.13204A>G