Canonical Allele Identifier: PA2499278439
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1179011
ClinVar RCV Id: RCV001535820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Cys2042Tyr
CA387523850
NM_014363.6:c.6125G>A