Canonical Allele Identifier: PA658664502
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 449520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro536Leu
CA387547599
NM_014363.6:c.1607C>T