Canonical Allele Identifier: PA2826577858
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1050150
ClinVar RCV Id: RCV001357115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu2821Phe
CA387515621
NM_001278055.2:c.8461C>T