Canonical Allele Identifier: PA2499278509
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1176616
ClinVar RCV Id: RCV001532229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His3458Tyr
CA387512359
NM_014363.6:c.10372C>T