Canonical Allele Identifier: PA2580354825
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2031949
ClinVar RCV Id: RCV002876619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp3236Glu
CA387513834
NM_014363.6:c.9708C>G
CA387513835
NM_014363.6:c.9708C>A