Canonical Allele Identifier: PA645437506
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Val2389Met
CA6910961
NM_014363.6:c.7165G>A