Canonical Allele Identifier: PA2826578231
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2908204
ClinVar RCV Id: RCV003751338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Glu3339Asp
CA6910448
NM_001278055.2:c.10017A>C
CA387512170
NM_001278055.2:c.10017A>T