Canonical Allele Identifier: PA1139731961
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 969206
ClinVar RCV Id: RCV001244500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His3575Leu
CA387511560
NM_014363.6:c.10724A>T