Canonical Allele Identifier: PA094481
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 554337
ClinVar RCV Id: RCV000669953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn4549Asp
CA387504800
NM_014363.6:c.13645A>G