Canonical Allele Identifier: PA1139730121
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 848646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala433Pro
CA6911933
NM_014363.6:c.1297G>C