Canonical Allele Identifier: PA658808575
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 527996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asn1586Ser
CA6911347
NM_014363.6:c.4757A>G