Canonical Allele Identifier: PA916014213
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 648020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp3402Gly
CA6910487
NM_014363.6:c.10205A>G