Canonical Allele Identifier: PA2580355088
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2109127
ClinVar RCV Id: RCV003019926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His4292Pro
CA6910059
NM_014363.6:c.12875A>C