Canonical Allele Identifier: PA2580354565
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2177416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Val2060Ala
CA6911120
NM_014363.6:c.6179T>C