Canonical Allele Identifier: PA2826578390
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 619025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Trp3554Arg
CA6910340
NM_001278055.2:c.10660T>C
CA387510733
NM_001278055.2:c.10660T>A