Canonical Allele Identifier: PA2826578062
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 284017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu3097His
CA10604661
NM_001278055.2:c.9290T>A