Canonical Allele Identifier: PA916014065
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 649183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Gln2137Glu
CA6911086
NM_014363.6:c.6409C>G