Canonical Allele Identifier: PA645437650
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311508
ClinVar RCV Id: RCV000392204 RCV000518679 RCV000633069 RCV001573868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile3632Met
CA6910375
NM_014363.6:c.10896A>G