Canonical Allele Identifier: PA2580355101
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2191754
ClinVar RCV Id: RCV002620762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro4342Leu
CA387506170
NM_014363.6:c.13025C>T