Canonical Allele Identifier: PA2826576632
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 180208
ClinVar RCV Id: RCV000157061
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser1050Pro
CA273726
NM_001278055.2:c.3148T>C