Canonical Allele Identifier: PA2826576603
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2176060
ClinVar RCV Id: RCV002582194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro1011Ser
CA6911516
NM_001278055.2:c.3031C>T