Canonical Allele Identifier: PA2573090670
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1343977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ser4389Ala
CA387505861
NM_014363.6:c.13165T>G