Canonical Allele Identifier: PA645437195
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp315Gly
CA6912001
NM_014363.6:c.944A>G