Canonical Allele Identifier: PA2580354771
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2092189
ClinVar RCV Id: RCV003015986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Tyr3071Cys
CA6910652
NM_014363.6:c.9212A>G