Canonical Allele Identifier: PA658664600
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448208
ClinVar RCV Id: RCV001276941 RCV002473033 RCV002525073 RCV002527519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Trp1861Cys
CA6911227
NM_014363.6:c.5583G>C
CA387525353
NM_014363.6:c.5583G>T