Canonical Allele Identifier: PA658664551
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448201
ClinVar RCV Id: RCV000517613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Gly1116Cys
CA387535743
NM_014363.6:c.3346G>T