Canonical Allele Identifier: PA2580355061
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2179813
ClinVar RCV Id: RCV002615240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Gln4226Leu
CA6910111
NM_014363.6:c.12677A>T