Canonical Allele Identifier: PA658808505
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 528018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp324Glu
CA6911995
NM_014363.6:c.972C>A
CA387550632
NM_014363.6:c.972C>G