Canonical Allele Identifier: PA1139731041
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 994455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile2260Val
CA6911033
NM_014363.6:c.6778A>G