Canonical Allele Identifier: PA1139732038
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 938832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile3706Val
CA6910338
NM_014363.6:c.11116A>G