Canonical Allele Identifier: PA2826577316
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp2046Asn
CA6911059
NM_001278055.2:c.6136G>A