Canonical Allele Identifier: PA2826578120
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 582271
ClinVar RCV Id: RCV000706307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys3172Glu
CA387513291
NM_001278055.2:c.9514A>G