Canonical Allele Identifier: PA645437484
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311534
ClinVar RCV Id: RCV000286135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Leu2151Val
CA10639233
NM_014363.6:c.6451T>G