Canonical Allele Identifier: PA2580354739
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2073363
ClinVar RCV Id: RCV002944035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro2935Ser
CA387515825
NM_014363.6:c.8803C>T