Canonical Allele Identifier: PA2826576737
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1256214
ClinVar RCV Id: RCV001663556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro1225Ala
CA387532423
NM_001278055.2:c.3673C>G