Canonical Allele Identifier: PA2826577709
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1972852
ClinVar RCV Id: RCV002750408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Met2597Ile
CA387517087
NM_001278055.2:c.7791G>T
CA387517088
NM_001278055.2:c.7791G>C
CA387517089
NM_001278055.2:c.7791G>A