Canonical Allele Identifier: PA2826576204
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2751507
ClinVar RCV Id: RCV003589482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Phe406Leu
CA6911873
NM_001278055.2:c.1218C>G
CA387547345
NM_001278055.2:c.1218C>A
CA387547358
NM_001278055.2:c.1216T>C